4.5 Article

Quantitative determination of major alkaloids in areca nut products by high-performance liquid chromatography coupled with ion mobility spectrometry

Journal

JOURNAL OF SEPARATION SCIENCE
Volume 45, Issue 24, Pages 4469-4477

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/jssc.202200361

Keywords

areca nut; arecaidine; arecoline; guvacine; high-performance liquid chromatography; ion mobility spectrometry

Funding

  1. National Natural Science Foundation of China [21864021]
  2. Science and Technology Plan Project of Hunan Province, China [2019RS1058, 21A0091]

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In this study, a high-performance liquid chromatography coupled with an ion mobility spectrometer method was developed for sensitive determination of areca alkaloids in areca nut samples. The method utilized an X-Bridge C-18 column and a custom-made post-column splitter, which successfully overcame the difficulty of detecting areca alkaloids using traditional UV detectors and improved the quantitative performance of high-performance liquid chromatography.
Areca nut is a popular and addictive food as well as a traditional herbal medicine in many countries. Areca nut contains alkaloids including arecoline, guvacine, and arecaidine, which are the major bioactive compounds in areca products. Areca alkaloids can be carcinogenic, and thus sensitive and specific analytical methods are urgently desired for the identification and quantification of these compounds. High-performance liquid chromatography-based methods are often preferred, but areca alkaloids do not have chromophores, and detection using a traditional UV detector can be difficult. The complexity of areca sample extracts can also lead to the co-elution of peaks leading to poor quantitative performance. We report here high-performance liquid chromatography coupled with an ion mobility spectrometer for sensitive determination of areca alkaloids in various products including areca nut, areca nut products, and herbal oral liquid. An X-Bridge reversed-phase C-18 column was used in the experiment and was combined with high-performance liquid chromatography coupled to an ion mobility spectrometer system. A custom-made adjustable post-column splitter acted as an interface between the high-performance liquid chromatography and the ion mobility spectrometer; it also acted as the electrospray ionization source. The mobile phase was methanol and 0.5% ammonium hydroxide. The results demonstrate that the splitter can afford a wide range of split ratios that match the ion mobility spectrometer ionization source while keeping the separation efficiency of high-performance liquid chromatography. Three major alkaloid compounds were then accurately determined using the resulting method without dativization steps. Many coeluted high-performance liquid chromatography peaks are effectively separated in the ion mobility spectrometer dimension, which in turn improved the quantification accuracy.

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